Rhodococcus and application of rhodococcus in degradation of lignin
A rhodococcus and lignin technology, applied in the field of microorganisms, can solve problems such as difficult degradation, environmental pollution, and chemical methods cannot solve pollution problems, and achieve low cost and no secondary pollution
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Embodiment 1
[0021] Rhodococcus ( Rhodococcus sp.) L17 was isolated and purified from sea mud in the South China Sea.
[0022] The separation and purification method is as follows: the acclimatization medium used is inorganic salt medium, and the composition is (g / L): 6.2g Na 2 HPO 4 , 3.0g KH 2 PO 4 , 0.5g NaCl, 1.0g NH 4 Cl, pH 7.0. First, add 3g of sludge to 100mL of inorganic salt medium containing 20mg / L lignin, and after acclimatization at 37°C for 60 days, insert 10% inoculum volume of lignin into inorganic salt medium containing 40mg / L of lignin, and then acclimate for one week, followed by By analogy, gradually increase the concentration of lignin for domestication, and the concentrations of lignin are 40mg / L, 60mg / L, and 80mg / L respectively.
[0023] After the acclimatization, spread the acclimatization solution on the agar plate (beef extract 3g / L, peptone 10g / L, sodium chloride 5g / L, agar powder 20g / L, pH7.0) and culture at 37°C for 48h, and select a single colony on Be...
Embodiment 2
[0034] Rhodococcus ( Rhodococcus sp.) L17 single colony was inoculated in 3mL beef extract peptone medium, cultured for 18h (OD 600 0.45) with an inoculum volume of 20% by volume, insert it into an inorganic salt medium with a lignin concentration of 20mg / L and a pH of 8.0, react at 37°C with a shaker at 150rpm for 96h, and measure the degradation by UV spectrophotometry Rate. The mensuration of degradation rate is the same as embodiment 1, and detection result is that degradation rate is 78%.
Embodiment 3
[0036] Rhodococcus ( Rhodococcus sp. .) A single colony of L17 was inoculated in 3 mL of beef extract peptone medium, and the 18-hour culture was inserted into an inorganic salt medium with a lignin concentration of 60 mg / L and a pH of 7.0 at an inoculation volume of 40% by volume. ℃, 100rpm shaker reaction for 108h, the degradation rate was measured by ultraviolet spectrophotometry, the measurement method was the same as in Example 1, and the test result was that the degradation rate was 82%.
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